Opis choroby * EnglishPolish Pobierz sekcję do PDF Definicja A rare syndrome with combined immunodeficiency characterized by intrauterine and postnatal growth retardation, chronic neutropenia, and natural killer (NK) cell deficiency due a defect in DNA replication leading to blockade of immune cell differentiation in the bone marrow, particularly affecting NK cells. Other clinical features include recurrent viral and bacterial infections and eczema, as well as mild facial dysmorphism. Dane Klasyfikacja Choroba Synonimy CID due to GINS1 deficiency Combined immunodeficiency with intrauterine growth retardation-NK cell deficiency-neutropenia Combined immunodeficiency with intrauterine growth retardation-natural killer cell deficiency-neutropenia CID due to GINS1 deficiency Combined immunodeficiency with intrauterine growth retardation-NK cell deficiency-neutropenia Combined immunodeficiency with intrauterine growth retardation-natural killer cell deficiency-neutropenia Kod ORPHA 505227 Kod OMIM 617827 Kod ICD10 D81.8 Kod ICD11 4A01.1Y *Źródło Rozszerzony opis choroby Pobierz sekcję do PDF Brak opisu rozszerzonego dla tej choroby. Opracowanie w toku. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl